Cas 26142-98-3,Benzoic acid, 2-methyl-, 1,2-bis(2-methylphenyl)-1,2-ethenediyl ester, (E)-

26142-98-3

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Basic information

Product Name: Benzoic acid, 2-methyl-, 1,2-bis(2-methylphenyl)-1,2-ethenediyl ester, (E)-
Synonyms:
CAS NO:26142-98-3
Molecular Formula: C32H28O4
Molecular Weight: 476.572
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzoic acid, 2-methyl-, 1,2-bis(2-methylphenyl)-1,2-ethenediyl ester, (E)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 2-methyl-, 1,2-bis(2-methylphenyl)-1,2-ethenediyl ester, (E)-(26142-98-3)
EPA Substance Registry System: Benzoic acid, 2-methyl-, 1,2-bis(2-methylphenyl)-1,2-ethenediyl ester, (E)-(26142-98-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 26142-98-3(Hazardous Substances Data)

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26142-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26142-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,4 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26142-98:
(7*2)+(6*6)+(5*1)+(4*4)+(3*2)+(2*9)+(1*8)=103
103 % 10 = 3
So 26142-98-3 is a valid CAS Registry Number.

26142-98-3Upstream product

20045-96-9 o-methylbenzoyl bromide

26142-98-3Downstream Products

26142-98-3Relevant academic research and scientific papers

Electroreductive coupling of aromatic acyl bromides to 1,2-diketones

Kise,Ueda

, p. 755 - 756 (2001)

The direct electroreduction of aromatic acyl bromides gave aromatic 1,2-diketones. The best result was obtained using a Pb cathode in acetonitrile containing Bu4NClO4 as a supporting electrolyte. Aromatic acyl bromides substituted by an electron-donating group afforded 1,2-diketones in moderate-to-good yields, whereas acylated endiols were formed exclusively from aromatic acyl bromides substituted by an electron-withdrawing group.

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